Bioscience, Biotechnology, and Biochemistry
Online ISSN : 1347-6947
Print ISSN : 0916-8451
Organic Chemistry Regular Papers
Synthesis of 1,2-Oxygenated 6-arylfurofuran Lignan: Stereoselective Synthesis of (1S,2S,5R,6S)-1-hydroxysamin
Satoshi YAMAUCHISatoshi BANDOYoshiro KINOSHITA
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2002 Volume 66 Issue 7 Pages 1495-1499

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Abstract

  (1S,2S,5R,6S )-6-(3,4-Methylenedioxyphenyl)-3,7-dioxabicyclo[3.3.0]octan-1,2-diol ((+)-1-hydroxysamin 1) was synthesized, starting from olefin 8. Stereoselective α-hydroxylation was achieved after converting 8 to aldehyde 13. Resulting unstable α-hydroxy aldehyde 14 was then transformed to (+)-1-hydroxysamin (1). This is a new efficient synthetic route to 1,2-oxygenated 6-arylfurofuran lignans.

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© 2002 by Japan Society for Bioscience, Biotechnology, and Agrochemistry
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